Jg. Sheng et al., MICROGLIAL INTERLEUKIN-1-ALPHA EXPRESSION IN BRAIN-REGIONS IN ALZHEIMERS-DISEASE - CORRELATION WITH NEURITIC PLAQUE DISTRIBUTION, Neuropathology and applied neurobiology, 21(4), 1995, pp. 290-301
Interleukin-1 alpha-immunoreactive (IL-1 alpha(+)) microglia are promi
nent components of neuritic plaques in Alzheimer's disease, and may be
important in the evolution of neuritic plaques from diffuse amyloid d
eposits. Neuritic plaques show a characteristic distribution across ce
rebral regions and are absent in the cerebellum of patients with Alzhe
imer's disease. We used single- and dual-immunohistochemical labelling
to investigate the possibility that the expression of IL-1 alpha is c
orrelated with this regional distribution of neuritic (tau 2-immunorea
ctive, tau 2(+)) plaques. In Alzheimer's disease, tau 2(+) neuritic pl
aques occurred with increasing frequency in grey matter of frontal and
occipital lobes temporal lobe, and hippocampus. There were positive p
rominent components of neuritic plaques in correlations between the re
gional patterns of distribution of activated IL-1 alpha(+) microglia a
nd tau2(+) neuritic plaques as well as between activated IL-1 alpha(+)
microglia and activated astrocytes. No activated lL-1 alpha(+) microg
lia, tau 2(+) neuritic plaques, or activated astrocytes were observed
in cerebellum of these Alzheimer patients. These regional relationship
s between activated IL-1 alpha(+) microglia, tau 2(+) neuritic plaques
, and activated astrocytes; together with the established functions of
IL-1, support a causal association between the overexpression of IL-1
and the evolution of beta-amyloid deposits into neuritic plaques in A
lzheimer's disease.